The invention generally relates to synthetic mimics of cell penetrating peptides. More particularly, the invention relates to certain novel monomers, oligomers and polymers (e.g., co-polymers) that are useful for the preparation of synthetic mimics of cell penetrating peptides, their compositions, preparations and use.

Disclosed are self-assembling diblock copolymers of the formula (I): ##STR00001##
wherein R.sup.1-R.sup.4, n, and m are as described herein, which find use in preparing self-assembled structures and porous membranes. Embodiments of the self-assembled structures contain the diblock copolymer in a cylindrical morphology. Also disclosed is a method of preparing such copolymers.

Disclosed herein is a composition comprising a block copolymer; where the block copolymer comprises a first polymer and a second polymer; where the first polymer and the second polymer of the block copolymer are different from each other and the block copolymer forms a phase separated structure; an additive polymer; where the additive polymer comprises a bottle brush polymer; where the bottle brush polymer comprises a homopolymer that is the chemically and structurally the same as one of the polymers in the block copolymer or where the additive polymer comprises a graft copolymer that has a preferential interaction with one of the blocks of the block copolymers; and a solvent.

Aspects of the present disclosure generally describe polyarylether ketones and methods of use. In some aspects, a composition includes one or more polymers of formulae (I), (II), or (III):

##STR00001##

A novel monomer design for the synthesis of PPE-type polymers containing conjugated segments of well-defined length connected by flexible linkers under Sonogashira reaction conditions is presented. The resulting polymers retain the photophysical properties of a fully conjugated PPE. The extent of incorporation of the flexible units along the backbone is governed by the comonomer feed ratio and can be varied in a statistically predictable fashion.

Disclosed is a block copolymer including: at least one block A not including any phosphonate group, and including at least one poly(alkylene oxide) group and at least one block B obtained by polymerization of a monomer B1 or of a mixture of monomers with ethylenic unsaturation including at least one monomer B1, wherein a monomer B1 is a monomer with ethylenic unsaturation including at least one phosphonate function,
to its preparation method by RAFT controlled radical polymerization and to its uses.

The present disclosure provides a white-light block polymer, an ink composition, and a manufacturing method thereof. The white-light block polymer makes it only necessary to print one ink when using inkjet printing, thereby simplifying inkjet printing processing and meanwhile preventing a crosstalk problem of pixels having different colors of light. The present disclosure makes the ink composition suitable for inkjet printing by properly mixing the white-light block polymer, an organic solvent, a surface tension modifier, and a viscosity modifier in a suitable ratio.

The invention discloses a block copolymer intrinsic stretchable electroluminescent elastomer and its preparation method and application. This type of elastomer is made from organic electroluminescent monomers, styrene and 1,3-butadiene through anionic polymerization. The innovation of the present invention is: for the first time, the organic electroluminescence unit is introduced into the elastomer by chemical crosslinking. On the basis of improving the intrinsic stretchability of the elastomer, at the same time, it has characteristics of excellent luminescence and high carrier mobility, novel structure and unique design strategy; meanwhile, it also solves the inherent non-stretchability problem of traditional organic optoelectronic materials and the problem that traditional elastomers do not have electroluminescent properties. This type of elastomer is used as a light-emitting layer material to prepare organic electroluminescent devices with high stability, high stretchability and high efficiency.

In an aspect, a method of synthesizing a graft copolymer comprises the steps of: copolymerizing a first macromonomer and a first reactive diluent; wherein said first macromonomer comprises a first backbone precursor directly or indirectly covalently linked to a first polymer side chain group; wherein said reactive diluent is provided in the presence of the first macromonomer at an amount selected so as to result in formation said graft copolymer having a first backbone incorporating said diluent and said first macromonomer in a first polymer block characterized by a preselected first graft density or a preselected first graft distribution of said first macromonomer. In some embodiments of this aspect, said preselected first graft density is any value selected from the range of 0.05 to 0.75. In some methods, the composition and amount of said diluent is selected to provide both a first preselected first graft density and a first preselected first graft distribution.

The present invention discloses a terpolymer based on 2,5-bis(2-thienyl)thiazolo[5,4-d]thiazolyl. In the invention, by introducing 2,5-bis(2-thienyl)thiazolo[5,4-d]thiazole units, the conjugated length of the polymers is enlarged and the aggregation in solution becomes weak. The introducing of 2,5-bis(2-thienyl)thiazolo[5,4-d]thiazole unit can easily tune the photophysical properties and the aggregation structure of the terploymers, and the terpolymers show excellent photovoltaic performance. The terpolymers have the following general formula:

##STR00001##